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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MECR
Duplication
(splice donor variant +1 more)
Dystonia, childhood-onset, with optic atrophy and basal ganglia abnormalities
+2 more
GPathogenic/Likely pathogenic
OPA1
(R626H +8 more)
Single nucleotide variant
(missense variant)
OPA1-related condition
+1 more
GUncertain significance